| Systematic (IUPAC) name | |
|---|---|
| (2S,3S,4R,6S)-6-{[(2R,3S,4R,5R,6S)-4-(dimethylamino)-5-hydroxy-6-{[(4R,6S,7R,9R,10R,11E,13E,16R)-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-4-(propanoyloxy)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy}-2-methyloxan-3-yl]oxy}-4-hydroxy-2,4-dimethyloxan-3-yl propanoate | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 35457-80-8 |
| ATC code | J01FA03 |
| PubChem | CID 5382853 |
| ChemSpider | 4445365 |
| UNII | N34Z0Y5UH7 |
| KEGG | D01339 |
| Chemical data | |
| Formula | C41H67NO15 |
| Mol. mass | 813.968 g/mol |
| SMILES | eMolecules & PubChem |
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| Physical data | |
| Melt. point | 155–156 °C (311–313 °F) |
| Solubility in water | Soluble in acidic/low pH water; Very soluble in methanol, chloroform, ethyl acetate, benzene, ethyl ether; Almost completely in ethanol(>95.5) mg/mL (20 °C) |
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Midecamycin is a macrolide antibiotic. Synthesized from Streptomyces mycarofaciens.
Melting point vary depending on the compound type. It may also vary depending on the source consulted. Example:
For the A1 type:
The Merck Index reports 155-156 Celsius. The Japanese Pharmacopoeia reports 153–158 Celsius.
For the A3 type:
The Merck Index reports 122-125 Celsius.
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